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Gut microbiome reflect adaptation of earthworms to cave and surface environments

BACKGROUND: Caves are special natural laboratories for most biota and the cave communities are unique. Establishing population in cave is accompanied with modifications in adaptability for most animals. To date, little is known about the survival mechanisms of soil animals in cave environments, albe...

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Autores principales: Gong, Xin, Chen, Ting-Wen, Zhang, Lili, Pižl, Václav, Tajovský, Karel, Devetter, Miloslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356433/
https://www.ncbi.nlm.nih.gov/pubmed/35932082
http://dx.doi.org/10.1186/s42523-022-00200-0
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author Gong, Xin
Chen, Ting-Wen
Zhang, Lili
Pižl, Václav
Tajovský, Karel
Devetter, Miloslav
author_facet Gong, Xin
Chen, Ting-Wen
Zhang, Lili
Pižl, Václav
Tajovský, Karel
Devetter, Miloslav
author_sort Gong, Xin
collection PubMed
description BACKGROUND: Caves are special natural laboratories for most biota and the cave communities are unique. Establishing population in cave is accompanied with modifications in adaptability for most animals. To date, little is known about the survival mechanisms of soil animals in cave environments, albeit they play vital roles in most terrestrial ecosystems. Here, we investigated whether and how gut microbes would contribute to the adaptation of earthworms by comparing the gut microbiome of two earthworm species from the surface and caves. RESULTS: Two dominant earthworm species inhabited caves, i.e., Allolobophora chlorotica and Aporrectodea rosea. Compared with the counterparts on the surface, A. rosea significantly decreased population in the cave, while A. chlorotica didn’t change. Microbial taxonomic and phylogenetic diversities between the earthworm gut and soil environment were asynchronic with functional diversity, with functional gene diversity been always higher in earthworm gut than in soil, but species richness and phylogenetic diversity lower. In addition, earthworm gut microbiome were characterized by higher rrn operon numbers and lower network complexity than soil microbiota. CONCLUSIONS: Different fitness of the two earthworm species in cave is likely to coincide with gut microbiota, suggesting interactions between host and gut microbiome are essential for soil animals in adapting to new environments. The functional gene diversity provided by gut microbiome is more important than taxonomic or phylogenetic diversity in regulating host adaptability. A stable and high-efficient gut microbiome, including microbiota and metabolism genes, encoded potential functions required by the animal hosts during the processes of adapting to and establishing in the cave environments. Our study also demonstrates how the applications of microbial functional traits analysis may advance our understanding of animal-microbe interactions that may aid animals to survive in extreme ecosystems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-022-00200-0.
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spelling pubmed-93564332022-08-07 Gut microbiome reflect adaptation of earthworms to cave and surface environments Gong, Xin Chen, Ting-Wen Zhang, Lili Pižl, Václav Tajovský, Karel Devetter, Miloslav Anim Microbiome Research Article BACKGROUND: Caves are special natural laboratories for most biota and the cave communities are unique. Establishing population in cave is accompanied with modifications in adaptability for most animals. To date, little is known about the survival mechanisms of soil animals in cave environments, albeit they play vital roles in most terrestrial ecosystems. Here, we investigated whether and how gut microbes would contribute to the adaptation of earthworms by comparing the gut microbiome of two earthworm species from the surface and caves. RESULTS: Two dominant earthworm species inhabited caves, i.e., Allolobophora chlorotica and Aporrectodea rosea. Compared with the counterparts on the surface, A. rosea significantly decreased population in the cave, while A. chlorotica didn’t change. Microbial taxonomic and phylogenetic diversities between the earthworm gut and soil environment were asynchronic with functional diversity, with functional gene diversity been always higher in earthworm gut than in soil, but species richness and phylogenetic diversity lower. In addition, earthworm gut microbiome were characterized by higher rrn operon numbers and lower network complexity than soil microbiota. CONCLUSIONS: Different fitness of the two earthworm species in cave is likely to coincide with gut microbiota, suggesting interactions between host and gut microbiome are essential for soil animals in adapting to new environments. The functional gene diversity provided by gut microbiome is more important than taxonomic or phylogenetic diversity in regulating host adaptability. A stable and high-efficient gut microbiome, including microbiota and metabolism genes, encoded potential functions required by the animal hosts during the processes of adapting to and establishing in the cave environments. Our study also demonstrates how the applications of microbial functional traits analysis may advance our understanding of animal-microbe interactions that may aid animals to survive in extreme ecosystems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-022-00200-0. BioMed Central 2022-08-05 /pmc/articles/PMC9356433/ /pubmed/35932082 http://dx.doi.org/10.1186/s42523-022-00200-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Gong, Xin
Chen, Ting-Wen
Zhang, Lili
Pižl, Václav
Tajovský, Karel
Devetter, Miloslav
Gut microbiome reflect adaptation of earthworms to cave and surface environments
title Gut microbiome reflect adaptation of earthworms to cave and surface environments
title_full Gut microbiome reflect adaptation of earthworms to cave and surface environments
title_fullStr Gut microbiome reflect adaptation of earthworms to cave and surface environments
title_full_unstemmed Gut microbiome reflect adaptation of earthworms to cave and surface environments
title_short Gut microbiome reflect adaptation of earthworms to cave and surface environments
title_sort gut microbiome reflect adaptation of earthworms to cave and surface environments
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356433/
https://www.ncbi.nlm.nih.gov/pubmed/35932082
http://dx.doi.org/10.1186/s42523-022-00200-0
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